Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2
Tropospheric 18 O 18 O is an emerging proxy for past tropospheric ozone and free-tropospheric temperatures. The basis of these applications is the idea that isotope-exchange reactions in the atmosphere drive 18 O 18 O abundances toward isotopic equilibrium. However, previous work used an offline box...
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ftdatacite:10.5281/zenodo.4763876 2023-05-15T16:39:28+02:00 Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 Yeung, Laurence 2021 https://dx.doi.org/10.5281/zenodo.4763876 https://zenodo.org/record/4763876 unknown Zenodo https://zenodo.org/communities/dryad https://dx.doi.org/10.1002/essoar.10506248.2 https://dx.doi.org/10.5061/dryad.c866t1g6t https://dx.doi.org/10.5281/zenodo.4763877 https://zenodo.org/communities/dryad Open Access MIT License https://opensource.org/licenses/MIT mit info:eu-repo/semantics/openAccess MIT Software SoftwareSourceCode article 2021 ftdatacite https://doi.org/10.5281/zenodo.4763876 https://doi.org/10.1002/essoar.10506248.2 https://doi.org/10.5061/dryad.c866t1g6t https://doi.org/10.5281/zenodo.4763877 2021-11-05T12:55:41Z Tropospheric 18 O 18 O is an emerging proxy for past tropospheric ozone and free-tropospheric temperatures. The basis of these applications is the idea that isotope-exchange reactions in the atmosphere drive 18 O 18 O abundances toward isotopic equilibrium. However, previous work used an offline box-model framework to explain the 18 O 18 O budget, approximating the interplay of atmospheric chemistry and transport. This approach, while convenient, has poorly characterized uncertainties. To investigate these uncertainties, and to broaden the applicability of the 18 O 18 O proxy, we developed a scheme to simulate atmospheric 18 O 18 O abundances (quantified as ∆ 36 values) online within the GEOS-Chem chemical transport model. These results are compared to both new and previously published atmospheric observations from the surface to 33 km. Simulations using a simplified O 2 isotopic equilibration scheme within GEOS-Chem show quantitative agreement with measurements only in the middle stratosphere; modeled ∆ 36 values are too high elsewhere. Investigations using a comprehensive model of the O-O 2 -O 3 isotopic photochemical system and proof-of-principle experiments suggest that the simple equilibration scheme omits an important pressure dependence to ∆ 36 values: the anomalously efficient titration of 18 O 18 O to form ozone. Incorporating these effects into the online ∆ 36 calculation scheme in GEOS-Chem yields quantitative agreement for all available observations. While this previously unidentified bias affects the atmospheric budget of 18 O 18 O in O 2 , the modeled change in the mean tropospheric ∆ 36 value since 1850 C.E. is only slightly altered; it is still quantitatively consistent with the ice-core ∆ 36 record, implying that the tropospheric ozone burden increased less than ~40% over the twentieth century. : Funding provided by: National Science Foundation Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000001 Award Number: AGS-2002422Funding provided by: National Science Foundation Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000001 Award Number: AGS-2002414Funding provided by: National Aeronautics and Space Administration Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000104 Award Number: NNX17AE36GFunding provided by: David and Lucile Packard Foundation Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000008 Award Number: Article in Journal/Newspaper ice core DataCite Metadata Store (German National Library of Science and Technology) |
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Tropospheric 18 O 18 O is an emerging proxy for past tropospheric ozone and free-tropospheric temperatures. The basis of these applications is the idea that isotope-exchange reactions in the atmosphere drive 18 O 18 O abundances toward isotopic equilibrium. However, previous work used an offline box-model framework to explain the 18 O 18 O budget, approximating the interplay of atmospheric chemistry and transport. This approach, while convenient, has poorly characterized uncertainties. To investigate these uncertainties, and to broaden the applicability of the 18 O 18 O proxy, we developed a scheme to simulate atmospheric 18 O 18 O abundances (quantified as ∆ 36 values) online within the GEOS-Chem chemical transport model. These results are compared to both new and previously published atmospheric observations from the surface to 33 km. Simulations using a simplified O 2 isotopic equilibration scheme within GEOS-Chem show quantitative agreement with measurements only in the middle stratosphere; modeled ∆ 36 values are too high elsewhere. Investigations using a comprehensive model of the O-O 2 -O 3 isotopic photochemical system and proof-of-principle experiments suggest that the simple equilibration scheme omits an important pressure dependence to ∆ 36 values: the anomalously efficient titration of 18 O 18 O to form ozone. Incorporating these effects into the online ∆ 36 calculation scheme in GEOS-Chem yields quantitative agreement for all available observations. While this previously unidentified bias affects the atmospheric budget of 18 O 18 O in O 2 , the modeled change in the mean tropospheric ∆ 36 value since 1850 C.E. is only slightly altered; it is still quantitatively consistent with the ice-core ∆ 36 record, implying that the tropospheric ozone burden increased less than ~40% over the twentieth century. : Funding provided by: National Science Foundation Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000001 Award Number: AGS-2002422Funding provided by: National Science Foundation Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000001 Award Number: AGS-2002414Funding provided by: National Aeronautics and Space Administration Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000104 Award Number: NNX17AE36GFunding provided by: David and Lucile Packard Foundation Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000008 Award Number: |
format |
Article in Journal/Newspaper |
author |
Yeung, Laurence |
spellingShingle |
Yeung, Laurence Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 |
author_facet |
Yeung, Laurence |
author_sort |
Yeung, Laurence |
title |
Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 |
title_short |
Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 |
title_full |
Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 |
title_fullStr |
Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 |
title_full_unstemmed |
Data reported in: Effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric O2 |
title_sort |
data reported in: effects of ozone isotopologue formation on the clumped-isotope composition of atmospheric o2 |
publisher |
Zenodo |
publishDate |
2021 |
url |
https://dx.doi.org/10.5281/zenodo.4763876 https://zenodo.org/record/4763876 |
genre |
ice core |
genre_facet |
ice core |
op_relation |
https://zenodo.org/communities/dryad https://dx.doi.org/10.1002/essoar.10506248.2 https://dx.doi.org/10.5061/dryad.c866t1g6t https://dx.doi.org/10.5281/zenodo.4763877 https://zenodo.org/communities/dryad |
op_rights |
Open Access MIT License https://opensource.org/licenses/MIT mit info:eu-repo/semantics/openAccess |
op_rightsnorm |
MIT |
op_doi |
https://doi.org/10.5281/zenodo.4763876 https://doi.org/10.1002/essoar.10506248.2 https://doi.org/10.5061/dryad.c866t1g6t https://doi.org/10.5281/zenodo.4763877 |
_version_ |
1766029811457720320 |